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Chemical Structure
Chemical Structure
Chemical Structure

Terbinafine hydrochloride [78628-80-5]

Research Use Only
CDX-T0207
Chemodex
CAS Number78628-80-5
Product group Chemicals
Estimated Purity>98%
Molecular Weight291.4 . 36.5
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Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    Terbinafine hydrochloride [78628-80-5]
  • Delivery Days Customer
    10
  • ADR Class
    9
  • CAS Number
    78628-80-5
  • Certification
    Research Use Only
  • Estimated Purity
    >98%
  • Hazard Information
    Excepted quantity,Warning
  • Molecular Formula
    C21H25N . HCl
  • Molecular Weight
    291.4 . 36.5
  • Scientific Description
    Chemical. CAS: 78628-80-5. Formula: C21H25N . HCl. MW: 291.4 . 36.5. Synthetic. Terbinafine is an antifungal and antimycotic compound that is highly active against dermatophytes, mold, other basic fungi, and some strains of yeast. It is clinically used to treat nail and skin infections. Inhibits ergosterol synthesis, essential component of fungal cell membranes. Potent non-competitive inhibitor at the stage of squalene epoxidation (IC50=30nM for C. albicans). Selective activator of the K2P channel TASK3 (pEC50 = 6.2). Exhibits >10-fold selectivity for TASK3 over TREK2, TRESK, THIK1 and TASK2. Also inhibits TWIK1 (pIC50 = 5.69). K2P channels might also be a target for ist antifungal activity. Shown to exhibit at higher concentrations anti-tumor and anti-angiogenic activity by inducing cell cycle arrest, and to display interesting anti-inflammatory and free radical scavenging activities. - Terbinafine is an antifungal and antimycotic compound that is highly active against dermatophytes, mold, other basic fungi, and some strains of yeast. It is clinically used to treat nail and skin infections. Inhibits ergosterol synthesis, essential component of fungal cell membranes. Potent non-competitive inhibitor at the stage of squalene epoxidation (IC50=30nM for C. albicans). Selective activator of the K2P channel TASK3 (pEC50 = 6.2). Exhibits >10-fold selectivity for TASK3 over TREK2, TRESK, THIK1 and TASK2. Also inhibits TWIK1 (pIC50 = 5.69). K2P channels might also be a target for ist antifungal activity. Shown to exhibit at higher concentrations anti-tumor and anti-angiogenic activity by inducing cell cycle arrest, and to display interesting anti-inflammatory and free radical scavenging activities.
  • SMILES
    CN(C/C=C/C#CC(C)(C)C)CC1=CC=CC2=CC=CC=C21.Cl
  • Storage Instruction
    2°C to 8°C,-20°C
  • UN Number
    3077
  • UNSPSC
    12352200